NDC 87441-011

Buprenorphine 2 mg tablet

On the label: Unit Dose Solutions, Inc.. It's repackaged: Unit Dose Solutions, Inc. rebottles it from Rhodes Pharmaceuticals L.P.'s NDC 42858-501.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Knoa Pharmaceuticals LLCWilson, NC, United StatesMakes it Problems found, fixed voluntarilySep 26, 2025 · 9 inspections

Repackaging site

Product details

Generic drug
Buprenorphine: every company that makes it
Form
tablet, sublingual
Strength
2 mg
Approval
ANDA ANDA207276
On the market since
Jun 17, 2026
Package NDCs
87441-011-01
Official label
DailyMed (National Library of Medicine), updated Jun 17, 2026

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